University of Chicago Medicine Inflammatory Bowel Disease Center, Chicago, Illinois.
Department of Pathology, University of Chicago, Chicago, Illinois.
Clin Gastroenterol Hepatol. 2018 Jan;16(1):68-74. doi: 10.1016/j.cgh.2017.07.023. Epub 2017 Jul 26.
BACKGROUND & AIMS: Patients with primary sclerosing cholangitis (PSC) and ulcerative colitis (UC) have a high risk of colonic neoplasia. Neoplasia frequently develops in the proximal colon in patients with PSC. Histologic inflammation is an independent risk factor for the development of neoplasia; we investigated whether patients with UC and PSC have more subclinical disease activity than patients with UC alone.
We performed a retrospective analysis of data from 143 patients (205 examinations) with ulcerative pancolitis who were in clinical remission and treated at a tertiary medical center from May 2011 through May 2016. Endoscopic and histologic activity were compared between patients with PSC (from 36 examinations) and without PSC (from 169 examinations). Disease activity was scored per colonic segment using a modified Mayo endoscopic subscore and histologic assessment. In each colonic segment, differences in disease activity and the degree of discordance between endoscopic and histologic inflammation among UC patients with and without PSC were compared.
Patients with UC-PSC had significantly more subclinical endoscopic (odds ratio [OR], 4.21; 95% CI, 1.67-10.63) and histologic activity (OR, 5.13; 95% CI, 2.25-11.68) in the right colon, as well as greater degree of histologic than endoscopic inflammation in the proximal colon (OR, 3.14, 95% CI, 1.24-7.97), compared with patients without PSC. Patients with UC-PSC had significantly less histologic activity in the rectum on multivariate analysis (OR, 0.24; 95% CI, 0.08-0.72).
Patients with UC and PSC who are in clinical remission are significantly more likely to have endoscopic and histologic inflammation in the right colon than patients with UC without PSC. Our findings provide insight into cause of colorectal cancer in UC patients with PSC.
原发性硬化性胆管炎(PSC)和溃疡性结肠炎(UC)患者结直肠肿瘤的风险较高。PSC 患者的结直肠肿瘤常发生在近端结肠。组织学炎症是肿瘤发生的独立危险因素;我们研究了 PSC 和 UC 并存的患者是否比单纯 UC 患者有更多的亚临床疾病活动。
我们对 2011 年 5 月至 2016 年 5 月在一家三级医疗中心接受治疗的处于临床缓解期的 143 例(205 次检查)溃疡性全结肠炎患者的数据进行了回顾性分析。比较了 PSC 患者(36 次检查)和无 PSC 患者(169 次检查)的内镜和组织学活动。采用改良的 Mayo 内镜亚评分和组织学评估对每段结肠的疾病活动进行评分。比较了 UC 患者中有无 PSC 时各段结肠的疾病活动和内镜与组织学炎症之间的不相符程度。
UC-PSC 患者的右半结肠有显著更多的亚临床内镜(优势比[OR],4.21;95%可信区间[CI],1.67-10.63)和组织学活动(OR,5.13;95%CI,2.25-11.68),近端结肠的组织学炎症程度大于内镜炎症(OR,3.14;95%CI,1.24-7.97),而无 PSC 的患者则没有。多变量分析显示,UC-PSC 患者的直肠组织学活动显著减少(OR,0.24;95%CI,0.08-0.72)。
处于临床缓解期的 UC 和 PSC 并存的患者,其右半结肠发生内镜和组织学炎症的可能性明显高于单纯 UC 患者。我们的研究结果为 UC 合并 PSC 患者结直肠癌的病因提供了新的见解。